Canonical Allele Identifier: PA2826012945
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1065175
ClinVar RCV Id: RCV001375623

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Arg1181Trp
CA349056089
NM_001165964.3:c.3541A>T